These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 22383218)

  • 1. Screening of congenital heart disease patients using multiplex ligation-dependent probe amplification: early diagnosis of syndromic patients.
    Sørensen KM; El-Segaier M; Fernlund E; Errami A; Bouvagnet P; Nehme N; Steensberg J; Hjortdal V; Soller M; Behjati M; Werge T; Kirchoff M; Schouten J; Tommerup N; Andersen PS; Larsen LA
    Am J Med Genet A; 2012 Apr; 158A(4):720-5. PubMed ID: 22383218
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Analysis of gene copy number variations in patients with congenital heart disease using multiplex ligation-dependent probe amplification.
    Mutlu ET; Aykan HH; Karagöz T
    Anatol J Cardiol; 2018 Jul; 20(1):9-15. PubMed ID: 29952356
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease.
    Zhang X; Xu Y; Liu D; Geng J; Chen S; Jiang Z; Fu Q; Sun K
    BMC Genomics; 2015 May; 16(1):364. PubMed ID: 25952753
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Copy number variants detection by microarray and multiplex ligation-dependent probe amplification in congenital heart diseases.
    Nagy O; Szakszon K; Biró BO; Mogyorósy G; Nagy D; Nagy B; Balogh I; Ujfalusi A
    J Biotechnol; 2019 Jun; 299():86-95. PubMed ID: 31054299
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Pilot Study of Multiplex Ligation-Dependent Probe Amplification Evaluation of Copy Number Variations in Romanian Children with Congenital Heart Defects.
    Bolunduț AC; Nazarie F; Lazea C; Șufană C; Miclea D; Lazăr C; Mihu CM
    Genes (Basel); 2024 Feb; 15(2):. PubMed ID: 38397197
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genomic imbalances in syndromic congenital heart disease.
    Molck MC; Simioni M; Paiva Vieira T; Sgardioli IC; Paoli Monteiro F; Souza J; Fett-Conte AC; Félix TM; Lopes Monlléo I; Gil-da-Silva-Lopes VL
    J Pediatr (Rio J); 2017; 93(5):497-507. PubMed ID: 28336264
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Systemic Screening for 22q11.2 Copy Number Variations in Hungarian Pediatric and Adult Patients With Congenital Heart Diseases Identified Rare Pathogenic Patterns in the Region.
    Zodanu GKE; Oszlánczi M; Havasi K; Kalapos A; Rácz G; Katona M; Ujfalusi A; Nagy O; Széll M; Nagy D
    Front Genet; 2021; 12():635480. PubMed ID: 33995479
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects.
    Hussein IR; Bader RS; Chaudhary AG; Bassiouni R; Alquaiti M; Ashgan F; Schulten HJ; Al Qahtani MH
    Pediatr Cardiol; 2018 Jun; 39(5):924-940. PubMed ID: 29541814
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Multiplex ligation-dependent probe amplification analysis of GATA4 gene copy number variations in patients with isolated congenital heart disease.
    Guida V; Lepri F; Vijzelaar R; De Zorzi A; Versacci P; Digilio MC; Marino B; De Luca A; Dallapiccola B
    Dis Markers; 2010; 28(5):287-92. PubMed ID: 20592452
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Assessment of large copy number variants in patients with apparently isolated congenital left-sided cardiac lesions reveals clinically relevant genomic events.
    Hanchard NA; Umana LA; D'Alessandro L; Azamian M; Poopola M; Morris SA; Fernbach S; Lalani SR; Towbin JA; Zender GA; Fitzgerald-Butt S; Garg V; Bowman J; Zapata G; Hernandez P; Arrington CB; Furthner D; Prakash SK; Bowles NE; McBride KL; Belmont JW
    Am J Med Genet A; 2017 Aug; 173(8):2176-2188. PubMed ID: 28653806
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cytogenomic Evaluation of Subjects with Syndromic and Nonsyndromic Conotruncal Heart Defects.
    de Souza KR; Mergener R; Huber J; Campos Pellanda L; Riegel M
    Biomed Res Int; 2015; 2015():401941. PubMed ID: 26137477
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Rare de novo copy number variants in patients with congenital pulmonary atresia.
    Xie L; Chen JL; Zhang WZ; Wang SZ; Zhao TL; Huang C; Wang J; Yang JF; Yang YF; Tan ZP
    PLoS One; 2014; 9(5):e96471. PubMed ID: 24826987
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Burden of potentially pathologic copy number variants is higher in children with isolated congenital heart disease and significantly impairs covariate-adjusted transplant-free survival.
    Kim DS; Kim JH; Burt AA; Crosslin DR; Burnham N; Kim CE; McDonald-McGinn DM; Zackai EH; Nicolson SC; Spray TL; Stanaway IB; Nickerson DA; Heagerty PJ; Hakonarson H; Gaynor JW; Jarvik GP
    J Thorac Cardiovasc Surg; 2016 Apr; 151(4):1147-51.e4. PubMed ID: 26704054
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Copy number variations in the GATA4, NKX2-5, TBX5, BMP4 CRELD1, and 22q11.2 gene regions in Chinese children with sporadic congenital heart disease.
    Li Z; Huang J; Liang B; Zeng D; Luo S; Yan T; Liao F; Huang J; Li J; Cai R; Deng X; Tang N
    J Clin Lab Anal; 2019 Feb; 33(2):e22660. PubMed ID: 30221396
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Screening of copy number variants in the 22q11.2 region of congenital heart disease patients from the São Miguel Island, Azores, revealed the second patient with a triplication.
    Pires R; Pires LM; Vaz SO; Maciel P; Anjos R; Moniz R; Branco CC; Cabral R; Carreira IM; Mota-Vieira L
    BMC Genet; 2014 Nov; 15():115. PubMed ID: 25376777
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Copy number variant analysis for syndromic congenital heart disease in the Chinese population.
    Li P; Chen W; Li M; Zhao Z; Feng Z; Gao H; Suo M; Xu Z; Tian G; Wu F; Wei S; Huang G
    Hum Genomics; 2022 Oct; 16(1):51. PubMed ID: 36316717
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Combined G-banded karyotyping and multiplex ligation-dependent probe amplification for the detection of chromosomal abnormalities in fetuses with congenital heart defects].
    Liu Y; Xie J; Geng Q; Xu Z; Wu W; Luo F; Li S; Wang Q; Chen W; Tan H; Zhang H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):1-5. PubMed ID: 28186583
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease.
    Warburton D; Ronemus M; Kline J; Jobanputra V; Williams I; Anyane-Yeboa K; Chung W; Yu L; Wong N; Awad D; Yu CY; Leotta A; Kendall J; Yamrom B; Lee YH; Wigler M; Levy D
    Hum Genet; 2014 Jan; 133(1):11-27. PubMed ID: 23979609
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of chromosome 22q11 copy number variations by multiplex ligation-dependent probe amplification for prenatal diagnosis of congenital heart defect.
    Zhang J; Ma D; Wang Y; Cao L; Wu Y; Qiao F; Liu A; Li L; Lin Y; Liu G; Liu C; Hu P; Xu Z
    Mol Cytogenet; 2015; 8():100. PubMed ID: 26715944
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Detection of copy number variations in pediatric ETV6/RUNX1-positive acute lymphoblastic leukemia with multiplex ligation-dependent probe amplification].
    Zhang L; Liu XM; Guo Y; Yang WY; Zhang JY; Liu F; Liu TF; Wang SC; Chen XJ; Ruan M; Qi BQ; Chang LX; Zou Y; Chen YM; Zhu XF
    Zhongguo Dang Dai Er Ke Za Zhi; 2016 Jan; 18(1):34-8. PubMed ID: 26781410
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.